Detalhe da pesquisa
1.
Involvement of the JAK-STAT pathway in the molecular landscape of tyrosine kinase fusion-negative hypereosinophilic syndromes: A nationwide CEREO study.
Am J Hematol
; 99(6): 1108-1118, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38563187
2.
High frequency of clonal hematopoiesis in Erdheim-Chester disease.
Blood
; 137(4): 485-492, 2021 01 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33067622
3.
Genetic identification of patients with AML older than 60 years achieving long-term survival with intensive chemotherapy.
Blood
; 138(7): 507-519, 2021 08 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34410352
4.
Mutational profile and benefit of gemtuzumab ozogamicin in acute myeloid leukemia.
Blood
; 135(8): 542-546, 2020 02 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31880804
5.
Clonal interference of signaling mutations worsens prognosis in core-binding factor acute myeloid leukemia.
Blood
; 132(2): 187-196, 2018 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29692343
6.
Association of fludarabin, cytarabine, and fractioned gemtuzumab followed by hematopoietic stem cell transplantation for first-line refractory acute myeloid leukemia in children: A single-center experience.
Pediatr Blood Cancer
; 67(6): e28305, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32307866
7.
Three UBA1 clones for a unique VEXAS syndrome.
Rheumatology (Oxford)
; 63(2): e48-e50, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37698981
8.
Poor prognosis of chromosome 7 clonal aberrations in Philadelphia-negative metaphases and relevance of potential underlying myelodysplastic features in chronic myeloid leukemia.
Haematologica
; 104(6): 1150-1155, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30573507
9.
Comprehensive mutational profiling of core binding factor acute myeloid leukemia.
Blood
; 127(20): 2451-9, 2016 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-26980726
10.
Germline PAX5 mutation predisposes to familial B-cell precursor acute lymphoblastic leukemia.
Blood
; 137(10): 1424-1428, 2021 03 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33036026
11.
Leon's helmet.
Haematologica
; 108(5): 1450-1451, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36226490
12.
Clinical relevance of IDH1/2 mutant allele burden during follow-up in acute myeloid leukemia. A study by the French ALFA group.
Haematologica
; 103(5): 822-829, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29472349
13.
Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia.
Eur J Haematol
; 100(1): 104-107, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29034503
14.
Diagnostic challenge in a case of ambiguous lineage acute leukemia with PICALM::MLLT10 rearrangement.
Pediatr Blood Cancer
; 70(11): e30573, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37439579
15.
Inherited transmission of the CSF3R T618I mutational hotspot in familial chronic neutrophilic leukemia.
Blood
; 134(26): 2414-2416, 2019 12 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31697825
16.
Germline pathogenic variants in transcription factors predisposing to pediatric acute myeloid leukemia: results from the French ELAM02 trial.
Haematologica
; 106(3): 908-912, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32554555
17.
Comprehensive molecular landscape in patients older than 80 years old diagnosed with acute myeloid leukemia: A study of the French Hauts-de-France AML observatory.
Am J Hematol
; 94(1): E24-E27, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30358899
18.
Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA.
Am J Hematol
; 89(6): 610-5, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24616160
19.
Down syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome.
Haematologica
; 103(6): e274-e276, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29217785
20.
UBTF tandem duplications define a distinct subtype of adult de novo acute myeloid leukemia.
Leukemia
; 37(6): 1245-1253, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37085611